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Blood. 2017 Nov 2;130(18):1995-2005. doi: 10.1182/blood-2017-04-778779. Epub 2017 Aug 29.

Uncovering the mystery of opposite circadian rhythms between mouse and human leukocytes in humanized mice.

Author information

1
Institute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore.
2
Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
3
Department of Pathology and Laboratory Medicine, Kandang Kerbau (KK) Women's and Children's Hospital, Singapore.
4
Duke-National University of Singapore Graduate Medical School, Singapore.
5
Department of Obstetrics & Gynaecology, KK Women's and Children's Hospital, Singapore; and.
6
Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Abstract

Many immune parameters show circadian rhythms during the 24-hour day in mammals. The most striking circadian oscillation is the number of circulating immune cells that display an opposite rhythm between humans and mice. The physiological roles and mechanisms of circadian variations in mouse leukocytes are well studied, whereas for humans they remain unclear because of the lack of a proper model. In this study, we found that consistent with their natural host species, mouse and human circulating leukocytes exhibited opposite circadian oscillations in humanized mice. This cyclic pattern of trafficking correlated well with the diurnal expression levels of C-X-C chemokine receptor 4, which were controlled by the intracellular hypoxia-inducible factor 1α/aryl hydrocarbon receptor nuclear translocator-like heterodimer. Furthermore, we also discovered that p38 mitogen-activated protein kinases/mitogen-activated 2 had opposite effects between mice and humans in generating intracellular reactive oxygen species, which subsequently regulated HIF-1α expression. In conclusion, we propose humanized mice as a robust model for human circadian studies and reveal insights on a novel molecular clock network in the human circadian rhythm.

PMID:
28851698
DOI:
10.1182/blood-2017-04-778779
[Indexed for MEDLINE]

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